Canonical Allele Identifier: CA766892649

Gene: CAPN10

Linked Data

• dbSNP Id: rs1308142891
• MyVariant Identifiers: chr2:g.241542643A>C (hg19) ; chr2:g.240603226A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240603226A>C , CM000664.2:g.240603226A>C	GRCh38
NC_000002.11:g.241542643A>C , CM000664.1:g.241542643A>C	GRCh37
NC_000002.10:g.241191316A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000270364.11:c.274-13162A>C	ENSP00000270364.7:n.274-13162A>C
ENST00000426297.1:c.167-3161A>C